DAZL 抗体 (AA 51-130)
(1 reference)-
- 抗原 See all DAZL 抗体
- DAZL (Deleted in Azoospermia-Like (DAZL))
-
抗原表位
- AA 51-130
-
适用
- 小鼠, 绵羊
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This DAZL antibody is un-conjugated
-
应用范围
- Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunocytochemistry (ICC)
- 交叉反应
- 小鼠, 绵羊
- 预测反应
- Human,Dog,Cow,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human DAZL
- 亚型
- IgG
- Top Product
- Discover our top product DAZL Primary Antibody
-
anti-Deleted in Azoospermia-Like (DAZL) (AA 186-295) antibody
DAZL 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Deleted in Azoospermia-Like (DAZL) (Internal Region) antibodyVerified DAZL 适用: 大鼠 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Deleted in Azoospermia-Like (DAZL) (AA 130-250) antibodyDAZL 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Deleted in Azoospermia-Like (DAZL) (N-Term) antibodyDAZL 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Deleted in Azoospermia-Like (DAZL) (AA 1-295) antibodyDAZL 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Deleted in Azoospermia-Like (DAZL) (AA 218-267) antibodyDAZL 适用: 人, 小鼠, 大鼠, Pig, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Deleted in Azoospermia-Like (DAZL) (C-Term) antibodyDAZL 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Deleted in Azoospermia-Like (DAZL) (C-Term) antibodyDAZL 适用: 人, 小鼠, 大鼠, Cow, 犬, 山羊, 豚鼠, 马, 兔 WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 - 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
-
-
: "Decrease in male mouse fertility by hydrogen sulfide and/or ammonia can Be inheritable." in: Chemosphere, Vol. 194, pp. 147-157, (2018) (PubMed).
-
: "Decrease in male mouse fertility by hydrogen sulfide and/or ammonia can Be inheritable." in: Chemosphere, Vol. 194, pp. 147-157, (2018) (PubMed).
-
- 抗原
- DAZL (Deleted in Azoospermia-Like (DAZL))
- 别名
- DAZL (DAZL 产品)
- 别名
- DAZH antibody, DAZL1 antibody, DAZLA antibody, SPGYLA antibody, DAZL antibody, Xdazl antibody, dazh antibody, dazl1 antibody, dazla antibody, spgyla antibody, dazl-B antibody, dazl-a antibody, Daz-like antibody, Dazh antibody, Dazl1 antibody, Dazla antibody, Tpx-2 antibody, Tpx2 antibody, deleted in azoospermia like antibody, deleted in azoospermia-like antibody, deleted in azoospermia-like L homeolog antibody, DAZL antibody, dazl antibody, Dazl antibody, dazl.L antibody
- 背景
-
Synonyms: DAZ homolog, DAZ like autosomal, DAZ-like autosomal, deleted in azoospermia-like, DAZH, DAZL 1, DAZL, DAZL_HUMAN, DAZL1, DAZLA, Deleted in azoospermia like 1, Deleted in azoospermia like, Deleted in azoospermia like autosomal, Deleted in azoospermia-like 1, Deleted in azoospermia-like, Germline specic RNA binding protein, MGC26406, Spermatogenesis gene on the Y like autosomal, SPGY like autosomal, SPGY-like-autosomal, SPGYLA, Tpx2.
Background: The DAZ (Deleted in AZoospermia) gene family encodes potential RNA binding proteins that are expressed in prenatal and postnatal germ cells of males and females. The protein encoded by this gene is localized to the nucleus and cytoplasm of fetal germ cells and to the cytoplasm of developing oocytes. In the testis, this protein is localized to the nucleus of spermatogonia but relocates to the cytoplasm during meiosis where it persists in spermatids and spermatozoa. Transposition and amplification of this autosomal gene during primate evolution gave rise to the DAZ gene cluster on the Y chromosome. Mutations in this gene have been linked to severe spermatogenic failure and infertility in males. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010].
- 基因ID
- 1618
-
