CA5A Polyclonal antibody

CA5A Polyclonal Antibody for IF/ICC, ELISA
Cat No. 22241-1-AP

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

IF/ICC, ELISA

CA VA, CA5, Carbonate dehydratase VA, Carbonic anhydrase 5A, mitochondrial, Carbonic anhydrase VA

Formulation:  PBS, Azide, Glycerol
PBS, Azide, Glycerol
Conjugate:  Unconjugated
Unconjugated
Size/Concentration: 

-/ -


ご購入について

国内販売は「コスモ・バイオ株式会社」を通じて行っております。お見積り・ご注文はお近くの販売代理店へご連絡ください。


国内在庫・納期について

約2万点のプロテインテック製品をコスモバイオ社物流センター(国内)に在庫しています。国内在庫の有無はコスモバイオ社ホームページの「品番検索」でカタログ番号を検索して確認できます。


保証・サポートについて

テクニカルサポートまたはご購入後1年間の交換/補填対応を承ります。詳細はこちらをご覧ください。


Tested Applications

Positive IF/ICC detected inHeLa cells

Recommended dilution

ApplicationDilution
Immunofluorescence (IF)/ICCIF/ICC : 1:200-1:800
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

22241-1-AP targets CA5A in IF/ICC, ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

CatNo: Ag17689

Product name: Recombinant human CA5A protein

Source: e coli.-derived, PET28a

Tag: 6*His

Domain: 77-126 aa of BC137411

Sequence: DPQLKPLRVSYEAASCLYIWNTGYLFQVEFDDATEASGISGGPLENHYRL

相同性解析による交差性が予測される生物種
Full Name carbonic anhydrase VA, mitochondrial
Calculated molecular weight 305 aa, 35 kDa
GenBank accession numberBC137411
Gene Symbol CA5A
Gene ID (NCBI) 763
RRIDAB_3742068
Conjugate Unconjugated
Form
FormLiquid
Purification MethodAntigen affinity purification
UNIPROT IDP35218
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol{{ptg:BufferTemp}}7.3
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

Background Information

Carbonic anhydrase VA (CA-VA) is a mitochondrial enzyme that is highly expressed in the liver and functions to provide bicarbonate as a substrate for other enzymatic reactions.CA-VA deficiency , which is caused by biallelic pathogenic variants in the CA5A gene, is characterized by neonatal metabolic hyperammonemic encephalopathy, lactic acidosis, hypoglycemia, and ketonuria. (PMID: 41113665, PMID: 24530203)

Protocols

Product Specific Protocols
IF protocol for CA5A antibody 22241-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols
Loading...
||
New chat

Able

正在加载,请稍候...